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rs796053083

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796053083(-;-)
Make rs796053083(-;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165994177
GeneLOC102724058, SCN1A
is asnp
is mentioned by
dbSNPrs796053083
ebirs796053083
HLIrs796053083
Exacrs796053083
Varsomers796053083
Maprs796053083
PheGenIrs796053083
hapmaprs796053083
1000 genomesrs796053083
hgdprs796053083
ensemblrs796053083
gopubmedrs796053083
geneviewrs796053083
scholarrs796053083
googlers796053083
pharmgkbrs796053083
gwascentralrs796053083
openSNPrs796053083
23andMers796053083
23andMe allrs796053083
SNP Nexus

SNPshotrs796053083
SNPdbers796053083
MSV3drs796053083
GWAS Ctlgrs796053083
Max Magnitude0
ClinVar
Risk rs796053083(;)
Alt rs796053083(;)
Reference rs796053083(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene LOC102724058 SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166850687delA
CLNSRC
CLNACC RCV000189063.1,